Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939936Generated: November 1, 2026

Chlorotrimethylsilane → HCID 21465245, compound

https://huagongshe.com/reaction/1939936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantHCID 53706251HCID 53706251—
SolventTolueneHCID 1140—
ProductHCID 21465245HCID 21465245153.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

330 mg of 6-(1-isoquinolyloxy)-4-methoxymethyl-β-carboline-3-carboxylic acid isopropyl ester is mixed in 10 ml of toluene with 0.62 ml of triethylamine and 0.2 chlorotrimethylsilane and heated for 45 minutes to a bath temperature of 50°-60° C. After concentration by evaporation to about 6 ml, it is cooled to -78° C. under argon and 1.25 ml of a 1.2 molar diisobutyl aluminum hydride is instilled in hexane. After 30 minutes at -78° C., it is mixed with 3 ml of ethanol and 0.75 ml of 1N NaOH. It is mixed with ethyl acetate and very little water. The organic phase is separated and concentrated by evaporation without drying. The residue is mixed with hexane and yields 440 mg of 6-(1-isoquinolyloxy)-4-methoxymethyl-β-carboline-3-carbaldehyde. 254 mg of it is mixed in 2.5 ml of dimethylfuran with 67.5 mg of hydroxylamine hydrochloride and 69 mg of potassium hydroxide powder and allowed to stand for 16 hours at room temperature. The batch is poured on ice and the precipitate is suctioned off and rewashed with water. 133 mg of 6-(1-isoquinolyloxy-4-methoxymethyl-β-carboline-3-carbaldehyde oxime of melting point 215°-218° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05698555
Source datasetuspto-grants-1997_12
ORD IDord-589a0793e319487badae099084478a82
Source noteuspto-grants-1997_12