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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226605Generated: November 2, 2026

Chlorotrimethylsilane → (S)-1-(10,11-dihydro-5H-dibenz [b,f]azepine-5-carbonyl)-4-(benzyloxycarbonyl)piperazine-2-carboxylic acid

https://huagongshe.com/reaction/2226605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantDiisopropylethylamineHCID 81531—
Reactant10,11-Dihydro-5H-dibenz[b,f]azepine-5-carbonyl chlorideHCID 118579—
Reactant(S)-4-(Benzyloxycarbonyl)piperazine-2-carboxylic acidHCID 1514273—
Product(S)-1-(10,11-dihydro-5H-dibenz [b,f]azepine-5-carbonyl)-4-(benzyloxycarbonyl)piperazine-2-carboxylic acidHCID 5411685424%

Reaction Steps

Following the procedure of Example 16, Step B, 811 mg (2.5 mmole) of (S)-4-(benzyloxycarbonyl)-piperazine-2-carboxylic acid (from Example 7, Step A) 680 mg (6.26 mmole) of chlorotrimethylsilane, 1.23 g (9.5 mmole) of N,N-diisopropylethylamine and 665 mg (2.5 mmole ) of 97% of 10,11-dihydro-5H-dibenz[b,f]-azepine-5-carbonyl chloride , gave 284 mg (24%) of (S)-1-(10,11-dihydro-5H-dibenz [b,f]azepine-5-carbonyl)-4-(benzyloxycarbonyl)piperazine-2-carboxylic acid, mp 185° C. (softened >90° C.); TLC Rf 0.68 (Antaltech SGF plates developed with isoamyl alcohol:acetone:water [5:2:1]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05348955
Source datasetuspto-grants-1994_09
ORD IDord-cebfff2dac744613adee8402d02ef427
Source noteuspto-grants-1994_09