Ammonium → tert-butyl 2-[1-(5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)spiro[2H-indole-3,4'-piperidine]-4-yl]pyrrolidine-1-carboxylate

HRID 1537850Notes

Reaction equation

HRID 1537850 reaction equation
[CH2:5]([c:6]1[cH:7][cH:8][cH:9][cH:10][cH:11]1)[N:12]1[CH2:13][CH2:14][C:15]2([CH2:16][N:17]([c:36]3[c:37]4[c:38]([n:39][cH:40][n:41]3)[CH2:42][CH2:43][CH:44]4[CH3:45])[c:18]3[cH:19][cH:20][cH:21][c:22]([CH:24]4[N:25]([C:29](=[O:30])[O:31][C:32]([CH3:33])([CH3:34])[CH3:35])[CH2:26][CH2:27][CH2:28]4)[c:23]32)[CH2:46][CH2:47]1.[CH3:48][OH:49].[CH:1]([O-:2])=[O:3].[NH4+:4]>>[NH:12]1[CH2:13][CH2:14][C:15]2([CH2:16][N:17]([c:36]3[c:37]4[c:38]([n:39][cH:40][n:41]3)[CH2:42][CH2:43][CH:44]4[CH3:45])[c:18]3[cH:19][cH:20][cH:21][c:22]([CH:24]4[N:25]([C:29](=[O:30])[O:31][C:32]([CH3:33])([CH3:34])[CH3:35])[CH2:26][CH2:27][CH2:28]4)[c:23]32)[CH2:46][CH2:47]1

Participants

5

Reactant 4

HCID 223AmmoniumHCID 283FormateHCID 887MethanolHCID 77568389HCID 77568389, compound

Product 1

HCID 77721663tert-butyl 2-[1-(5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)spiro[2H-indole-3,4'-piperidine]-4-yl]pyrrolidine-1-carboxylate

Sources & evidence

ORD record
ord-2baecbc314494375a164bccb2e2f55f7
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)

Reaction notes

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