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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353597Generated: October 30, 2026

Diisopropylethylamine → HCID 68452781, compound

https://huagongshe.com/reaction/2353597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant(1aS,5aR)-1,1,2-trimethyl-1,1a,5,5a-tetrahydro-3-thia-cyclopropa[a]pentalene-4-carboxylic acidHCID 57892448—
ReactantHCID 68454134HCID 68454134—
SolventFormic AcidHCID 284—
SolventDimethylformamideHCID 6228—
ProductHCID 68452781HCID 6845278150.4%

Reaction Steps

A solution of (1aS,5aR)-1,1,2-trimethyl-1,1a,5,5a-tetrahydro-3-thia-cyclopropa[a]pentalene-4-carboxylic acid (111 mg, 0.50 mmol), TBTU (177 mg, 0.55 mmol) and ethyl-diisopropylamine (282 μL, 1.65 mmol) in DMF (15 mL) is allowed to stand at rt for 20 min. A solution of 4-aminomethyl-2-methyl-phenol hydrochloride (96 mg, 0.55 mmol) and ethyl-diisopropylamine (94 μL, 0.55 mmol) in DMF (1.5 mL) is added and the mixture is allowed to stand at rt for 3 h. After the addition of formic acid (0.2 mL), the mixture is separated by HPLC to afford (1aS,5aR)-1,1,2-trimethyl-1,1a,5,5a-tetrahydro-3-thia-cyclopropa[a]pentalene-4-carboxylic acid 4-hydroxy-3-methyl-benzylamide (86 mg) as a colourless oil. LC-MS: tR=0.99 min, [M+1]+=342.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750040B2
Source datasetuspto-grants-2010_07
ORD IDord-5ca74a84ef54450f9bc6dba944dea5d5
Source noteuspto-grants-2010_07